rs13098911

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs13098911(C;T)

Make rs13098911(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

46193709

is a	snp
is	mentioned by
dbSNP	rs13098911
dbSNP (classic)	rs13098911
ClinGen	rs13098911
ebi	rs13098911
HLI	rs13098911
Exac	rs13098911
Gnomad	rs13098911
Varsome	rs13098911
LitVar	rs13098911
Map	rs13098911
PheGenI	rs13098911
Biobank	rs13098911
1000 genomes	rs13098911
hgdp	rs13098911
ensembl	rs13098911
geneview	rs13098911
scholar	rs13098911
google	rs13098911
pharmgkb	rs13098911
gwascentral	rs13098911
openSNP	rs13098911
23andMe	rs13098911
SNPshot	rs13098911
SNPdbe	rs13098911
MSV3d	rs13098911
GWAS Ctlg	rs13098911

GMAF

0.06015

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 20190752]
Trait	Celiac disease
Title	Multiple common variants for celiac disease influencing immune gene expression
Risk Allele	A
P-val	3E-17
Odds Ratio	1.30 [1.23-1.39]